• Collection, optimization and testing of new data analysis workflows and pipelines.
  • Basic statistics and quality assessment of sequencing outputs, quality trimming, removal of artifacts, read merging, etc.
  • Secondary data analysis using in-house standardized pipelines (the portfolio will increase in time):
    • Genome assembly and annotation;
    • Transcriptome assembly and annotation;
    • Resequencing, read mapping and variant detection;
    • Differential expression analysis and expression profiling;
    • Prediction of therapeutical effects of small molecules (Connectivity map concept);
    • Metagenomic analysis;
    • Phylogenetic analysis;
    • Analysis of SELEX, Ribosome display or Phague display libraries.
  • Custom data analysis based on existing standardized pipelines (e.g. workflows from literature).
  • Preparation of publication ready outputs in biopython and/or R.